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Exercise training in Diastolic Heart Failure (Ex‐ DHF ): rationale and design of a multicentre, prospective, randomized, controlled, parallel group trial
Author(s) -
Edelmann Frank,
Bobenko Anna,
Gelbrich Götz,
Hasenfuss Gerd,
HerrmannLingen Christoph,
Duvinage André,
Schwarz Silja,
Mende Meinhard,
Prettin Christiane,
Trippel Tobias,
Lindhorst Ruhdja,
Morris Daniel,
PieskeKraigher Elisabeth,
Nolte Kathleen,
Düngen HansDirk,
Wachter Rolf,
Halle Martin,
Pieske Burkert
Publication year - 2017
Publication title -
european journal of heart failure
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.149
H-Index - 133
eISSN - 1879-0844
pISSN - 1388-9842
DOI - 10.1002/ejhf.862
Subject(s) - medicine , heart failure , randomized controlled trial , physical therapy , heart failure with preserved ejection fraction , diastolic heart failure , quality of life (healthcare) , ejection fraction , diastole , cardiology , blood pressure , nursing
Heart failure with preserved ejection fraction ( HFpEF ) is a common disease with high incidence and increasing prevalence. Patients suffer from functional limitation, poor health‐related quality of life, and reduced prognosis. A pilot study in a smaller group of HFpEF patients showed that structured, supervised exercise training ( ET ) improves maximal exercise capacity, diastolic function, and physical quality of life. However, the long‐term effects of ET on patient‐related outcomes remain unclear in HFpEF . The primary objective of the Exercise training in Diastolic Heart Failure (Ex‐DHF) trial is to investigate whether a 12 month supervised ET can improve a clinically meaningful composite outcome score in HFpEF patients. Components of the outcome score are all‐cause mortality, hospitalizations, NYHA functional class, global self‐rated health, maximal exercise capacity, and diastolic function. After undergoing baseline assessments to determine whether ET can be performed safely, 320 patients at 11 trial sites with stable HFpEF are randomized 1:1 to supervised ET in addition to usual care or to usual care alone. Patients randomized to ET perform supervised endurance/resistance ET (3 times/week at a certified training centre) for 12 months. At baseline and during follow‐up, anthropometry, echocardiography, cardiopulmonary exercise testing, and health‐related quality of life evaluation are performed. Blood samples are collected to examine various biomarkers. Overall physical activity, training sessions, and adherence are monitored and documented throughout the study using patient diaries, heart rate monitors, and accelerometers. The Ex‐ DHF trial is the first multicentre trial to assess the long‐term effects of a supervised ET programme on different outcome measures in patients with HFpEF .

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